Postdoctoral work (with prof. H. Wennemers)
The AMI-isonitrile ligation 2.0: Fast, selective, and pH sensitive
Biedermann, M.‡; Markos, A.‡*, Warm, I., Schmitt, A., Heimgärtner, J.; Schmitt, A.; Lang, K.; Wennemers, H.*

Introducing Azomethine Imines to Chemical Biology: Bioorthogonal Reaction with Isonitriles
Markos, A.‡; Biedermann, M.‡; Heimgärtner, J.; Schmitt, A.; Lang, K.; Wennemers, H.*

Ph.D. work (with Dr. P. Beier)
Aza-Wolff Rearrangement of N-Fluoroalkyl Triazoles to Ketenimines
Kubíčková, A.; Markos, A.; Voltrová, S.; Marková, A.; Filgas, J.; Klepetářová, B.; Slavíček, P.; Beier, P.*

Lewis-Acid-Mediated Intramolecular Cyclization of 4-Aryl-5-Allyl-1,2,3-Triazoles to Substituted Cyclopentene Derivatives
Janecký, L.; Markos, A.; Klepetářová, B.; Beier, P.*

Fluoroalkyl Azides and Triazoles: Unlocking a
Novel Chemical Space
Markos, A.; Matoušek, V.; Beier, P.*

Ligand-dependent stereoselective Suzuki–Miyaura cross-coupling reactions of β-enamido triflates.
Chvojka, T.‡; Markos, A.‡; Voltrová, S.; Pohl, R.; Beier, P.*

Stereoselective Synthesis of (Z)-β-Enamido Fluorides from N-Fluoroalkyl-and N-Sulfonyl-1,2,3-Triazoles.
Markos, A.‡; Janecký, L.‡; Klepetářová, B.; Pohl, R.; Beier, P.*

Haloalkenyl Imidoyl Halides as Multifacial Substrates in the
Stereoselective Synthesis of N-Alkenyl Compounds
Markos, A.; Janecký, L.; Chvojka, T.; Martinek, T.; Martines-Seara, H.; Klepetářová, B.; Beier, P.*

General Approach to 2-Fluoroalkyl 1,3-Azoles via the Tandem Ring Opening and Defluorinative Annulation of N-Fluoroalkyl-1,2,3- Triazoles
Motornov, V.‡; Košťál, V.‡; Markos, A.‡; Täffner, D.; Beier, P.*

Stereoselective Synthesis of (Z)-β-Enamido Triflates and Fluorosulfonates from N-Fluoroalkylated Triazoles
Markos, A.; Voltrová, S.; Motornov, V.; Tichý, D.; Klepetářová, B.; Beier, P.*

A Rhodium-Catalyzed Transannulation of N-(per)Fluoroalkyl-1,2,3-Triazoles under Microwave Conditions – a General Route to N-(per)Fluoroalkyl-Substituted Five-Membered Heterocycles
Motornov, V. ‡; Markos, A. ‡; Beier, P.*
